肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2012年
12期
801-805
,共5页
潘翠萍%邵军%冯尧军%范威%吴新红%马彪
潘翠萍%邵軍%馮堯軍%範威%吳新紅%馬彪
반취평%소군%풍요군%범위%오신홍%마표
乳腺肿瘤%肿瘤干细胞%乙醛脱氢酶%生物学特性
乳腺腫瘤%腫瘤榦細胞%乙醛脫氫酶%生物學特性
유선종류%종류간세포%을철탈경매%생물학특성
Breast neoplasms%Tumor stem cells%Aldehyde dehydrogenases%Biological property
目的 证实人类乳腺癌MCF-7细胞系中存在乙醛脱氢酶阳性(ALDH+)乳腺癌干细胞,并研究ALDH+乳腺癌干细胞体外增殖、侵袭能力等生物学特性.方法 应用流式细胞术从MCF-7细胞中分离并培养ALDH+乳腺癌干/祖细胞,通过划痕试验、MTT法生长曲线测定以及Transwell法等检测ALDH+乳腺癌干细胞的生物学特性.结果 MCF-7细胞系中,CD-/low24CD+44细胞比例约为1.4%,ALDH+CD-/low24CD+44细胞比例约为1.2%;ALDH+乳腺癌干细胞与CD-/low24CD+44细胞的生长曲线基本一致;CD-/low24CD+44和ALDH+CD-/low24CD+44组细胞划痕区细胞间距离明显缩短,其迁移能力明显强于对照组,且两群干细胞之间存在差异;Transwell实验结果,与对照组相比,CD-/low24CD+44、ALDH+ CD-/low24CD+44两组细胞有大量细胞过膜,三组MTT检测吸光度值分别为1.05±0.098、1.56±0.075、1.67±0.032.结论 MCF-7细胞系中存在CD-/low24CD+44和ALDH+ CD-/low24CD+44乳腺癌干细胞,ALDH可作为鉴定乳腺癌干细胞的分子标志之一.
目的 證實人類乳腺癌MCF-7細胞繫中存在乙醛脫氫酶暘性(ALDH+)乳腺癌榦細胞,併研究ALDH+乳腺癌榦細胞體外增殖、侵襲能力等生物學特性.方法 應用流式細胞術從MCF-7細胞中分離併培養ALDH+乳腺癌榦/祖細胞,通過劃痕試驗、MTT法生長麯線測定以及Transwell法等檢測ALDH+乳腺癌榦細胞的生物學特性.結果 MCF-7細胞繫中,CD-/low24CD+44細胞比例約為1.4%,ALDH+CD-/low24CD+44細胞比例約為1.2%;ALDH+乳腺癌榦細胞與CD-/low24CD+44細胞的生長麯線基本一緻;CD-/low24CD+44和ALDH+CD-/low24CD+44組細胞劃痕區細胞間距離明顯縮短,其遷移能力明顯彊于對照組,且兩群榦細胞之間存在差異;Transwell實驗結果,與對照組相比,CD-/low24CD+44、ALDH+ CD-/low24CD+44兩組細胞有大量細胞過膜,三組MTT檢測吸光度值分彆為1.05±0.098、1.56±0.075、1.67±0.032.結論 MCF-7細胞繫中存在CD-/low24CD+44和ALDH+ CD-/low24CD+44乳腺癌榦細胞,ALDH可作為鑒定乳腺癌榦細胞的分子標誌之一.
목적 증실인류유선암MCF-7세포계중존재을철탈경매양성(ALDH+)유선암간세포,병연구ALDH+유선암간세포체외증식、침습능력등생물학특성.방법 응용류식세포술종MCF-7세포중분리병배양ALDH+유선암간/조세포,통과화흔시험、MTT법생장곡선측정이급Transwell법등검측ALDH+유선암간세포적생물학특성.결과 MCF-7세포계중,CD-/low24CD+44세포비례약위1.4%,ALDH+CD-/low24CD+44세포비례약위1.2%;ALDH+유선암간세포여CD-/low24CD+44세포적생장곡선기본일치;CD-/low24CD+44화ALDH+CD-/low24CD+44조세포화흔구세포간거리명현축단,기천이능력명현강우대조조,차량군간세포지간존재차이;Transwell실험결과,여대조조상비,CD-/low24CD+44、ALDH+ CD-/low24CD+44량조세포유대량세포과막,삼조MTT검측흡광도치분별위1.05±0.098、1.56±0.075、1.67±0.032.결론 MCF-7세포계중존재CD-/low24CD+44화ALDH+ CD-/low24CD+44유선암간세포,ALDH가작위감정유선암간세포적분자표지지일.
Objective To identify a aldehyde dehydrogenases positive (ALDH+) cancer stem cell subpopulation in MCF-7 cells and to investigate the proliferation and differentiation characteristics of these cells in vitro.Methods ALDH+ breast cancer stem cells were isolated from MCF-7 cells by flow cytometry and the biological property of ALDH+ breast cancer stem cells were examined by scarification test,MTT,growth curvature and Transwell migration assay.Results The ratio of CD-/low24 CD+44 cells was about 1.4 % in MCF-7 cells.The ratio of ALDH+ CD-/low24CD+44 cells was about 1.2 %.The growth curvature of ALDH+ breast cancer stem cells was almost the same with that of CD-/low24 CD+44 cells.The distance between cells was obviously shorter in both CD-/low24 CD+44 cells scarification zone and ALDH+ CD-/low24 CD+44 cells scarification zone.The migration ability of CD-/low24CD+44 cells and ALDH+ CD-/low24CD+44 cells was stronger than control group cells.There were migration ability differences between CD-/low24CD+44 cells and ALDH+ CD-/low24CD+44 cells.The results of Transwell experiments were in coincidence with above results.Lots of CD-/low24CD+44 cells and ALDH+ CD-/low24CD+44 cells were through the membrane.In MTT assay,absorbance values were 1.05±0.098,1.56±0.075 and 1.67±0.032.Conclusion CD--/low24CD+44 and ALDH+ CD-/low24CD+44 breast cancer stem cell subpopulation exist in MCF-7 cells.ALDH could potentially be used as a molecular marker to identify breast cancer stem cell subpopulation.